UBRO YELLOW MILKING COW INTRAMAMMARY SUSPENSION

Pajjiż: Irlanda

Lingwa: Ingliż

Sors: HPRA (Health Products Regulatory Authority)

Ixtrih issa

Ingredjent attiv:

PENETHAMATE HYDRIODIDE, DIHYDROSTREPTOMYCIN (AS THE SULFATE) PH. EUR., FRAMYCETIN SULFATE, PREDNISOLONE

Disponibbli minn:

Boehringer Ingelheim Ltd

Kodiċi ATC:

QJ51RV01

INN (Isem Internazzjonali):

PENETHAMATE HYDRIODIDE, DIHYDROSTREPTOMYCIN (AS THE SULFATE) PH. EUR., FRAMYCETIN SULFATE, PREDNISOLONE

Dożaġġ:

Unknown

Għamla farmaċewtika:

intramammary Suspension

Tip ta 'preskrizzjoni:

POM

Grupp terapewtiku:

Bovine

Żona terapewtika:

Antibacterials and corticosteroids

Indikazzjonijiet terapewtiċi:

Antibacterial

L-istatus ta 'awtorizzazzjoni:

Authorised

Data ta 'l-awtorizzazzjoni:

2006-02-10

Karatteristiċi tal-prodott

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Ubro Yellow Milking Cow Intramammary Suspension
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Intramammary suspension.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Bovine
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
The treatment of mastitis caused by organisms sensitive to penicillin, streptomycin or framycetin in milking cows.
4.3 CONTRAINDICATIONS
Do not use in animals with known hypersensitivity to the active ingredients.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
Each 5 ml dose unit contains the following active ingredients:
Penethamate hydriodide
150 mg
Dihydrostreptomycin (as the sulphate)
150 mg
Framycetin sulphate
50 mg
Prednisolone
5 mg
For a full list of excipients, see section 6.1
HEALTH PRODUCTS REGULATORY AUTHORITY
________________________________________________________________________________________________________________________
_Date Printed 07/12/2016_
_CRN 7023679_
_page number: 1_
4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
Before infusion, the teats should be thoroughly cleansed and disinfected and care should be taken to avoid contamination of
the injector nozzle. Following infusion it is advisable to use teat dip or spray.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE VETERINARY MEDICINAL PRODUCT TO ANIMALS
Penicillin and cephalosporins may cause hypersensitivity (allergy) following injection, inhalation, ingestion or skin
contact. Hypersensitivity to penicillin may lead to cross sensitivity to cephalosporins and vice versa. Allergic reaction to
these substances may occasionally be serious.
1.
Do not handle this product if you know you are sensitised or if you have been advised not to work with such
preparations.
2.
Handle this product
                                
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